doi: 10.3389/fmicb.2015.00259
Edited by: Aldo Corsetti, University of Teramo, Italy
Reviewed by: Giuseppe Spano, University of Foggia, Italy Giovanna Suzzi, Università degli Studi di Teramo, Italy
*Correspondence: Giulia Tabanelli, Interdepartmental Center for Industrial Agri-Food Research, University of Bologna, Piazza Goidanich 60, 47521 Cesena, FC, Italy giulia.tabanelli2@unibo.it
Specialty section: This article was submitted to Food Microbiology, a section of the journal Frontiers in Microbiology
Received: 16 February 2015 Accepted: 16 March 2015 Published: 10 April 2015 Citation: Bargossi E, Tabanelli G, Montanari C, Lanciotti R, Gatto V, Gardini F and Torriani S (2015) Tyrosine decarboxylase activity of enterococci grown in media with different nutritional potential: tyramine and 2-phenylethylamine accumulation and tyrDC gene expression. Front. Microbiol. 6:259. doi:10.3389/fmicb.2015.00259
Tyrosine decarboxylase activity of
enterococci grown in media with
different nutritional potential:
tyramine and 2-phenylethylamine
accumulation and tyrDC gene
expression
Eleonora Bargossi1,Giulia Tabanelli2*,Chiara Montanari2,Rosalba Lanciotti1,
Veronica Gatto3,Fausto Gardini1,2andSandra Torriani3
1Department of Agricultural and Food Sciences, University of Bologna, Cesena, Italy,2Interdepartmental Center for Industrial
Agri-Food Research, University of Bologna, Cesena, Italy,3Department of Biotechnology, University of Verona, Verona, Italy
The ability to accumulate tyramine and 2-phenylethylamine by two strains of
Enterococcus faecalis and two strains Enterococcus faecium was evaluated in two
cultural media added or not with tyrosine. All the enterococcal strains possessed a tyrosine decarboxylase (tyrDC) which determined tyramine accumulation in all the conditions tested, independently on the addition of high concentration of free tyrosine. Enterococci differed in rate and level of biogenic amines accumulation. E. faecalis EF37 and E. faecium FC12 produced tyramine in high amount since the exponential growth phase, while 2-phenylethylamine was accumulated when tyrosine was depleted. E.
faecium FC12 and E. faecalis ATCC 29212 showed a slower tyraminogenic activity
which took place mainly in the stationary phase up to 72 h of incubation. Moreover,
E. faecalis ATCC 29212 produced 2-phenylethylamine only in the media without
tyrosine added. In BHI added or not with tyrosine the tyrDC gene expression level differed considerably depending on the strains and the growth phase. In particular, the tyrDC gene expression was high during the exponential phase in rich medium for all the strains and subsequently decreased except for E. faecium FC12. Even if tyrDC presence is common among enterococci, this study underlines the extremely variable decarboxylating potential of strains belonging to the same species, suggesting strain-dependent implications in food safety.
Keywords: enterococci, tyramine, 2-phenylethylamine, tyrDC gene expression, intraspecific variability
Introduction
Tyramine is a biogenic amine (BA) deriving from the microbial decarboxylation of tyrosine. It can have severe acute effects if ingested in excessive amounts with food, causing an hypertensive syndrome known as “cheese reaction,” which consists in peripheral vasoconstriction, increased cardiac output, increased respiration, elevated blood glucose, and release of norepinephrine (McCabe-Sellers et al., 2006;Marcobal et al., 2012).
Lactic acid bacteria (LAB) are among the most efficient pro-ducers of tyrosine decarboxylase (tyrDC), the enzyme respon-sible for tyramine formation. In LAB, BA formation provides metabolic energy and/or acid resistance (Molenaar et al., 1993;
Fernández and Zúñiga, 2006). The presence of this enzyme is widespread among all LAB species (Marcobal et al., 2012). However, LAB belonging to the genus Enterococcus are rec-ognized as the most efficient tyramine producers (Suzzi and Gardini, 2003; Özogul and Özogul, 2007;Capozzi et al., 2011;
Kuley and Özogul, 2011;Ladero et al., 2012).
Tyramine production is considered a species characteristic of Enterococcus faecalis and also many strains of E. faecium possess this ability (Ladero et al., 2012). The E. faecalis tyrDC region was the first tyrDC locus described in prokaryotes (Connil et al., 2002). In E. faecalis, upstream the tyrDC gene, an ORF can be found (tyrS), responsible for a tyrosyl tRNA synthetase involved in an ATP-dependent activation of tyrosine by form-ing an enzyme-bound tyrosyl-adenylate intermediate (Marcobal et al., 2012). This tyrS could act as a sensor of the intracellu-lar tyrosine pool to regulate tyrosine decarboxylation (Linares et al., 2012). The ORF (tyrP) located downstream of tyrDC encodes a tyrosine-tyramine antiporter. The three genes are co-transcribed in some strain (Connil et al., 2002;Marcobal et al., 2012). In addition, in enterococci downstream of tyrP an ORF was found related to a gene encoding for an Na+/H+antiporter (nhaC-2) (Pessione et al., 2009; Marcobal et al., 2012). It has been demonstrated that the tyrDC of many tyraminogenic LAB, and especially enterococci, can decarboxylate, although with a lower efficiency, phenylalanine producing 2-phenylethylamine, a BA with characteristics very similar to tyramine (Marcobal et al., 2006).
Enterococci occur in many different habitats and, due to their association with the gastrointestinal tract, they are often contam-inant in food of animal origin (Franz et al., 2003, 2011). When present in the raw material, enterococci can survive to the fer-mentation process and can be found in fermented foods such as sausages and cheeses in which they can have a relevant role dur-ing ripendur-ing (Giraffa, 2003;Franz et al., 2011). Due to their salt and pH tolerance, as well as their ability to grow over a wide tem-perature range, these LAB are particularly competitive especially when the environmental conditions become harsher, and can be a relevant component of the ripening microbiota of fermented foods. Their beneficial technological properties and their positive impact on ripening and aroma formation in fermented sausages, cheeses, and olives are reported by several authors. In addition, some strains showed probiotic features, while many enterococci produce bacteriocins able to limit the growth of pathogenic and spoilage microorganisms (Fisher and Phillips, 2009;Franz et al., 2011).
On the other hand, enterococci are among the most common nosocomial pathogens and they can be responsible for endo-carditis, bacteremia, as well as urinary tract, central nervous system, intra-abdominal, and pelvic infections. In addition, ente-rococci are also known for their multiple antibiotic resistance (including vancomycin), which is in some case carried on mobile genetic elements transferable to other microorganisms (Klein, 2003). Moreover, several enterococci virulence factors have been
described, such as cytolysins, aggregation substances, and gelati-nase extracellular surface proteins (Foulquié Moreno et al., 2006). Finally, the presence of excessive content of tyramine in cheese and fermented meat is often attributed to these microorganisms (Joosten and Northolt, 1989;Suzzi and Gardini, 2003;Foulquié Moreno et al., 2006;Komprda et al., 2008).
The aim of this research was to study the tyramine and 2-phenylethylamine accumulation by four tyraminogenic strains of Enterococcus, two belonging to the species E. faecalis (EF37 and ATCC 29212) and two to the species E. faecium (FC12 and FC643). The ability to accumulate BAs was tested in a rich cultural medium, which does not limit enterococcal growth, and in a poor medium enhancing BA production (Bover-Cid and Holzapfel, 1999). Both media were tested with or with-out the addition of the precursor (tyrosine). In addition, the
tyrDC gene expression of the four enterococci was analyzed by
reverse transcription-quantitative real time PCR (RT-qPCR) dur-ing growth in rich medium in presence or not of the precursor.
Materials and Methods
Enterococcal Strains and Growth Conditions
The strains E. faecalis EF37 and ATCC 29212, E. faecium FC12, and FC643 were used in this work. E. faecalis EF37 and E. faecium FC12 were previously isolated from traditional Italian cheese while E. faecium FC643 were isolated from silage. The strains were stored in 20% (w/v) glycerol at−80◦C and pre-cultivated for 24 h at 37◦C in BHI Broth (Oxoid, Basingstoke, UK) added with 800 mg/l of tyrosine (Sigma–Aldrich, Gallarate, Italy).
After 24 h of pre-cultivation, the microorganisms were inocu-lated, at a concentration of approximately 6.5 log CFU/ml, in BHI Broth and in Bover-Cid and Holzapfel broth, a medium proposed to highlight the BA formation (BAM;Bover-Cid and Holzapfel, 1999), added or not with 800 mg/l of tyrosine and incubated at 37◦C for 96 h. At defined times (1, 2, 3, 4, 5, 6, 7, 8, 24, 48, 72, and 96 h), the changes of optical density at 600 nm (OD600)
were monitored. The modification of pH was determined by a pHmeter Basic 20 (Crison Instruments, Barcelona, Spain).
The maximum cell concentration reached in stationary phase was determined after 24 h of incubation by plate counting entero-cocci onto BHI agar. In addition, 2 ml aliquots of each culture was centrifuged at 3000 rpm for 10 min and the obtained cell pellets were frozen at−80◦C.
Growth Parameters
The evaluation of enterococcal growth in the different media was performed by measuring the OD600with a UV–VIS
spectropho-tometer (UV-1204, Shimadzu Corporation, Kyoto, Japan) with plastic cuvettes (1.5 ml). The OD600 data were fitted with the
Gompertz equation as modified byZwietering et al.(1990).
y= k + Ae−e[( μmaxe
A )(λ−t)+1]
where y is the OD600at time t, A represent the maximum OD600
value reached, μmax is the maximum OD600 increase rate in
Biogenic Amine Determination
The BA were determined after 4, 8, 24, 48, 72, and 96 h of incu-bation. The cultures were centrifuged at 10000 rpm for 10 min at 10◦C, and the supernatants were used for BAs determina-tion by HPLC after derivatizadetermina-tion with dansyl-chloride (Sigma– Aldrich, Gallarate, Italy) according toMartuscelli et al.(2000). The BA content was analyzed using a PU-2089 Intelligent HPLC quaternary pump, Intelligent UV–VIS multiwavelength detector UV 2070 Plus (Jasco Corporation, Tokio, Japan) and a man-ual Rheodyne injector equipped with a 20μl loop (Rheodyne, Rohnert Park, CA, USA). The quantification was performed according toTabanelli et al.(2012) and the amount tyramine and 2-phenylethylamine were expressed as mg/ml by reference to a calibration curve obtained with standard solutions.
Nucleic Acid Extraction from Enterococcal Cultures
Total DNA was isolated from cell pellets by using the Wizard Genomic DNA purification system (Promega Corporation, Madison, WI), following the manufacturer’s instructions.
For total RNA extraction, cells were washed twice with 500 μl of sterile diethyl pyrocarbonate (DEPC)-treated water and shaken three times at the maximum speed for 30 s at 10-s interval10-s with 500μl of LETS (200 mM LiCl, 20 mM EDTA, 20 mM Tris, 0,4% SDS, 0,1% DEPC), 500 mg of 450 μm-diameter glass beads (Sigma–Aldrich), 500 μl of phenol pH 4.7-chloroform-isoamyl alcohol (25:24:1 v/v; Sigma–Aldrich) in a cell disrupter (Mini-BeadBeater, BioSpec Products, Bartlesville, OK, USA). After centrifugation (4◦C, 13000 rpm, 10 min), the supernatant was twice treated with 600μl of chloroform-isoamyl alcohol (24:1 v/v; Sigma–Aldrich), added with 60 μl of 3 M sodium acetate, 1 ml of ice-cold absolute ethanol and left for 1 h at −80◦C. Total RNA was pelleted by centrifugation at 13000 rpm for 5 min at 4◦C, washed with 200 μl of ethanol 70%, and dissolved in 30μl of sterile water (RNAse- and DNAse-free).
DNA elimination was performed using 50 U of RNase-free DNase I recombinant (Roche Diagnostic, Germany) in 50μl of DNAse reaction buffer (40 mM Tris-HCl, 10 mM NaCl, 6 mM MgCl2, 1 mM CaCl2, pH 7.9) for 30 min at 25◦C. A PCR assay
was carried out to check for any contaminating DNA, and, when necessary, the DNase treatment was repeated.
DNA and RNA integrity, concentration, and purity were checked by electrophoresis on a 1,5% (wt/vol) agarose gel and by measurement with the NanoDropTM Lite Spectrophotometer (Thermo Fisher Scientific Inc., Waltham, MA, USA).
DNA and DNA-free RNA samples were stored at−20◦C and −80◦C, respectively, until use.
PCR Amplification and Expression of the
tyrDC Gene
A tyrDC fragment of about 336 bp was amplified using the primers DEC5 (5-CGT TGT TGG TGT TGT TGG CAC NAC NGA RGA RG-3) and DEC3 (5-CCG CCA GCA GAA TAT GGA AYR TAN CCC AT-3), following the PCR conditions described previously (Torriani et al., 2008). PCR product was visualized on a 2% agarose gel.
Total cDNA was synthesized from 1 μg of RNA using the ImProm-IITM Reverse Transcriptase kit (Promega, USA), fol-lowing the manufacturer’s recommendations.
The expression level of the tyrDC gene was analyzed by a RT-qPCR assay with primers TYR3f (5-CGT ACA CAT TCA GTT GCA TGG CAT-3) and TYR4r (5-ATG TCC TAC TTC TTC TTC CAT TTG-3); thermo cycler, reaction mixture, and amplifi-cation program were described inTorriani et al.(2008), as well as the procedure of the absolute quantification of the tyrDC copies number.
Statistical Analysis
The growth model was fitted using the statistical package Statistica for Windows 6.1 (Statsoft Italia, Vigonza, Italy).
Results
Growth and pH Modification in Cultural Media
The growth of four enterococcal strains, i.e., E. faecalis EF37 and ATCC 29212, and E. faecium FC12 and FC643, was monitored by measuring the OD600increase in the absence or in the presence
of tyrosine (800 mg/l) added in BHI and BAM media. The OD600
changes were modeled with the Gompertz equation (Zwietering et al., 1990) and the estimates of the parameters are reported in
Table 1.
When inoculated in BHI medium, all the strains reached the maximum value of OD600after 8 h of incubation at 37◦C,
inde-pendently on the presence of tyrosine. Given the high initial inoculums (about 6 log CFU/ml), the lag phase (λ) was always very short and it was followed by a sharp increase of OD600,
whose maximum values (estimated by the A parameter of the equation) ranged between 0.9 and 1.2. In particular, the absence of tyrosine favored the reaching of higher OD600values for the
two E. faecalis strains, and for E. faecium FC643. By contrast, no differences in the maximum OD600 were found for E. faecium
FC12 in relation to the presence of tyrosine added.
Table 1reports also the cell counts detected in the stationary phase (determined after 24 h incubation). In BHI no differences were detected in relation to the strain and to the addition of tyrosine. In fact, the counts revealed final cell concentrations comprised between 9.30 and 9.52 log CFU/ml.
All the strains, as expected, showed lower growth extent in BAM if compared with BHI. BAM is considered a poor medium and the energetic supply provided by aminoacid decarboxylation (and, consequently, by BA formation) became fundamental to support microbial growth. The more stringent conditions pro-vided by this medium are reflected also in the lower OD600
reached in the stationary phase. Anyway, the OD600was always
higher in the BAM not supplemented with tyrosine (Table 1). Also cell counts in stationary phase confirmed this behavior and were always higher in the medium without tyrosine, with the exception of the strain E. faecium FC643 in which no differences related to the presence of the aminoacid were found.
During incubation, the pH of the media was also monitored and the data are reported inFigure 1. The results in BHI were
TABLE 1 | Gompertz equation parameters for enterococcal growth measured as OD600.
Strain Cultural medium Gompertz equation parametersa R2 Residual mean square
error (RMSE)
Maximum cell concentration (log CFU/ml)
A μmax λ
EF37 BHI+ tyrb 0.947 0.767 2.532 0.977 0.042 9.40 (±0.13)
BHI 1.029 0.601 2.030 0.954 0.068 9.42 (±0.13)
BAM + tyrc 0.600 0.171 2.619 0.991 0.024 8.95 (±0.14)
BAM 0.803 0.192 2.121 0.993 0.031 9.04 (±0.11)
ATCC 29212 BHI+ tyr 0.899 0.494 2.399 0.989 0.013 9.30 (±0.15)
BHI 1.014 0.632 2.109 0.990 0.069 9.48 (±0.19) BAM+ tyr 0.544 0.191 3.455 0.989 0.049 8.52 (±0.15) BAM 0.788 0.252 2.544 0.992 0.043 8.80 (±0.14) FC12 BHI+ tyr 1.119 1.170 3.589 0.996 0.029 9.34 (±0.12) BHI 1.095 0.559 2.848 0.995 0.054 9.35 (±0.16) BAM+ tyr 0.362 0.132 1.882 0.989 0.037 8.33 (±0.14) BAM 0.425 0.124 2.077 0.993 0.039 8.31 (±0.17) FC643 BHI+ tyr 1.114 0.566 2.876 0.983 0.047 9.38 (±0.09) BHI 1.191 0.584 2.158 0.989 0.036 9.52 (±0.13) BAM+ tyr 0.739 0.177 1.635 0.992 0.028 8.46 (±0.20) BAM 0.807 0.187 1.445 0.993 0.028 8.72 (±0.11)
R2and RMSE are given as diagnostics of the regression. The maximum cell concentrations (expressed as log CFU/ml) at the beginning of the stationary phase is also reported.
aA, maximum OD600value reached;μmax, maximum OD600increase rate in exponential phase (OD600/h);λ, lag phase duration (h). bBHI Broth plus 800 mg/l tyrosine.
cBover-Cid and Holzapfel medium (BAM) plus 800 mg/l tyrosine.
specular to the growth curves for all the strains, and the pH decrease within the first 8 h was of about 1.5 units, and was quite constant during the remaining incubation period. In the samples added with tyrosine the pH value was higher of about 0.5 units, both at the beginning and at the end of incubation.
As far as BAM, the initial pH was 5.5 and only a slight decrease was observed in the first 8 h of incubation. This behavior can be attributed to the higher buffering potential of the medium. After the first 8 h, the pH showed a slight increase determined by the accumulation of BAs.
Biogenic Amine Production in the Cultural Media Not Added with Tyrosine
Both the media used for the trials contained, in different amount, aminoacid sources (proteins and peptides) among which precur-sors for tyrDC were present, allowing a decarboxylase activity of the strains also in the absence of tyrosine added. The amounts of tyramine and 2-phenylethylamine produced during the growth in these media are reported inFigures 2 and 3.
Enterococcus faecalis EF37 was able to produce tyramine in
both media. However, the final amount after 72 h did not exceed 70 mg/l in BHI and 90 mg/l in BAM (Figure 2A). These values did not significantly change prolonging the incubation up to 96 h (data not shown). The maximum tyramine concentration was observed in the samples taken after 24 h of incubation. Also 2-phenylethylamine was produced under the same conditions and this BA was gradually accumulated reaching a concentration of about 270 mg/l in BHI and 130 mg/l in BAM after 72 h. E.
fae-calis ATCC 29212 showed an analogous decarboxylating activity
even if lower tyramine amounts were produced in both media (Figure 2C).
A similar trend was observed for E. faecium FC12, though this strain accumulated in BHI higher concentrations of both the BAs while an opposite trend was observed for BAM (Figure 3A). Finally, E. faecalis FC643 showed the minor BA production in both the media and produced only traces of 2-phenylethylamine only in BHI (Figure 3C).
Biogenic Amine Production in the Cultural Media Added with Tyrosine
Figures 2 and 3report also the tyramine and 2-phenylethylamine accumulation when tyrosine (800 mg/l) was added to the two media. E. faecalis EF37 and E. faecium FC12 accumulated the maximum tyramine concentration within the first 8 h of incu-bation both in BHI and BAM and the reaching of the station-ary phase did not further increase significantly these amounts (Figures 2B and 3B,respectively).
Enterococcus faecalis EF37 was the most efficient strain in
the conversion of tyrosine to tyramine and the final concen-tration of this BA was about 515 mg/l in BHI and 620 mg/l in BAM. The behavior of E. faecium FC12 was similar, but the final amounts of tyramine were lower than E. faecalis EF37, i.e., 505 and 360 mg/l of BA were produced in BAM and BHI, respectively. In addition, both the strains began to produce 2-phenylethylamine only after 8 h of incubation, i.e., when sta-tionary phase and the maximum amount of tyramine have been reached. The 2-phenylethylamine accumulation increased during subsequent incubation and reached its maximum level at 72 h. About 513 and 428 mg/l of this amine were produced in BHI by
FIGURE 1 | Modification of the pH in BHI and Bover-Cid medium (BAM) with or without tyrosine. (A) E. faecalis EF37, (B) E. faecalis ATCC 29212, (C) E. faecium FC12, (D) E. faecium FC643.
E. faecium FC12 and E. faecalis EF37, respectively, while lower
concentrations were detected in BAM (about 230 mg/l for both the strains). In any case, these amounts were higher if compared with the 2-phenylethylamine produced in the same media in the absence of the tyrosine addition.
The presence of tyrosine determined a different behavior in the sample inoculated with E. faecalis ATCC 29212. Indeed, the growth of this strain was characterized by a slowed rate of accu-mulation of tyramine. This BA was mainly produced when the cells reached the stationary phase and amounts of about 325 and 510 mg/l were detected only after 72 h of incubation in BHI and BAM, respectively. In addition, no 2-phenylethylamine was pro-duced in both the conditions, even if this ability was displayed in the media without the addition of precursor (Figure 2D).
Enterococcus faecium FC643 showed a similar behavior and
reached in BAM a double concentration of tyramine with respect to BHI (592 mg/l vs. 288 mg/l). Also E. faecium FC643 did not accumulate 2-phenylethylamine when tyrosine was added to the media (Figure 3D).
Expression of the tyrDC Gene in BHI Added or Not with Tyrosine
All the enterococcal strains produced a 336-bp fragment char-acteristic of the tyrDC gene with the degenerate primers DEC5/DEC3 (data not shown), in accordance with their ability to accumulate tyramine. Therefore, the expression of the tyrDC gene could be evaluated by RT-qPCR during a period of 72 h. The expression of tyrDC gene has been evaluated during the enterococcal growth in BHI with or without tyrosine added.
As shown in Table 2, the tyrDC gene expression level dif-fered considerably depending on the the strains and the growth phase. In general, the two strains with the most effective tyra-minogenic activity showed since the beginning of incubation a level of transcript considerably higher than the other strains. It is important to note that the amount of tyrDC transcription is given as absolute value and the higher amount detected after 2 h did not correspond with the reaching of the maximum cell counts during incubation. Thus, the cell showed a considerably higher transcription activity during their early exponential phase.
Enterococcus faecalis EF37 displayed the highest level of tyrDC
transcription [up to 5–6 log (copies/μg cDNA)] during the expo-nential phase of growth (2–5 h) in both media, according with its great ability to accumulate tyramine. After that, a signif-icant decrease was found in BHI without tyrosine, while the
tyrDC mRNA was rather high in BHI added with tyrosine, thus
supporting the sequential 2-phenylethylamine production. The tyrDC gene expression of E. faecalis ATCC 29212 was always lower (about two log units in the first 8 h) if compared with E. faecalis EF37. Its expression was higher in BHI without added tyrosine at the beginning of the growth and transcription decreased drastically after 8 h.
The strain E. faecium FC12, although exhibiting a phenotypic behavior analogous to E. faecalis EF37, showed a very different trend of the tyrDC gene expression. Indeed, the transcript level in both media was not related to the phase of growth, but it was rather constant during the entire incubation period. For this strain the high level of transcript after 24 h could determine the increase of 2-phenylethyamine in both the media.
FIGURE 2 | Amounts of tyramine and 2-phenylethylamine produced during the growth in BHI and Bover-Cid medium (BAM) without (A,C) and with (B,D) tyrosine addition. (A,B) Enterococcus faecalis EF37, (C,D) E. faecalis ATCC 29212.
Finally, E. faecium FC643 exhibited a tyrDC gene expression behavior similar to E. faecalis ATCC 29212. However, it was char-acterized by the lowest levels of tyrDC transcription after 4 h of incubation.
Discussion
All the enterococcal strains used in these trials possessed an active tyrDC which determined tyramine accumulation (even if at dif-ferent level) in all the conditions tested, independently on the addition of high concentration of free tyrosine. This fact clearly indicated the possibility of the enterococci to decarboxylate amino acids present in the proteic and peptidic ingredients used for media preparation.
Recently, Liu et al. (2014a) showed that the activity of purified recombinant tyrDCs of the strains E. faecalis R612Z1 and E. faecium R615Z1 was similar, and that the enzymes exhibited higher specificity for tyrosine than for phenylalanine. However, in our trials, different behaviors of tyramine and 2-phenylethylamine accumulation were observed in relation to the strain. In particular, strains belonging to the same species (E.
faecalis or E. faecium) were characterized by different responses
indicating that, if the presence of tyrDC is common among enterococci, the decarboxylating potential can be extremely vari-able. The transcriptional analyses of the gene tyrDC confirmed these observations. In recent years, a number of studies have been conducted to evaluate the gene expression level of amino
acid decarboxylases on the BAs accumulation in different food and model systems (Gardini et al., 2008; Arena et al., 2011;
La Gioia et al., 2011; Rossi et al., 2011; Liu et al., 2014b). However, up to now no studies have compared the tyrDC tran-script levels in enterococcal strains of the same species. In the present study a variability of the tyrDC gene expression in dif-ferent strains of E. faecalis and E. faecium was evidenced for the first time. The two strains with the higher decarboxylat-ing potential (E. faecalis EF 37 and E. faecium FC12) were characterized by a higher transcription of tyrDC after 2 h of incubation and the maintenance of a remarkably higher tran-scription level throughout all the incubation period considered here.
In contrast with Arena et al. (2011), who observed an increase of tyrDC transcription in the presence of tyrosine for
Lactobacillus brevis IOEB 9809 in wine, in our conditions the
presence of the precursor in high amounts (800 mg/l) did not enhance the transcript at the beginning of growth, but stimulated a higher transcription during the successive incuba-tion.
Linares et al.(2009) evidenced that the maximization of the transcription of tyrDC and tyrP in E. durans was caused by a tyrosine concentration comprised between 2 and 5 mM. In this framework, the presence of tyramine added (800 mg/kg, i.e., 4.42 mM) should be sufficient to reach a high level of tyrDC transcript. Nevertheless, similar and often higher transcripts were obtained also in the medium without the addition of the precursor.
FIGURE 3 | Amounts of tyramine and 2-phenylethylamine produced during the growth in BHI and Bover-Cid medium (BAM) without (A,C) and with (B,D) tyrosine addition. (A,B) Enterococcus faecium FC12, (C,D) E. faecium FC643.
TABLE 2 | Tyrosine decarboxylase (tyrDC) gene expression level for enterococcal strains grown in BHI Broth and BHI Broth added with 800 mg/l tyrosine during 72 h.
Time (h) Log (copies/µg cDNA)
Enterococcus faecalis EF37 E. faecalis ATCC 29212 E. faecium FC12 E. faecium FC643
BHI BHI+ tyr BHI BHI+ tyr BHI BHI+ tyr BHI BHI+ tyr
2 5.08 (±0.02) 4.79 (±0.06) 3.11 (±0.07) 2.60 (±0.08) 4.98 (±0.22) 3.91 (±0.18) 3.86 (±0.02) 2.79 (±0.02) 4 4.87 (±0.01) 6.11 (±0.02) 3.06 (±0.14) 3.25 (±0.02) 3.45 (±0.01) 3.49 (±0.07) 2.19 (±0.11) 2.65 (±0.01) 8 5.22 (±0.05) 5.03 (±0.05) 2.23 (±0.09) 2.07 (±0.09) 3.37 (±0.42) 2.98 (±0.19) 1.98 (±0.25) 0.98 (±0.34) 24 2.42 (±0.07) 4.15 (±0.05) 1.10 (±0.45) 1.61 (±0.17) 3.42 (±0.07) 4.61 (±0.24) 1.65 (±0.29) 0.84 (±0.06) 48 2.81 (±0.03) 3.38 (±0.03) 1.02 (±0.04) 1.83 (±0.01) 3.08 (±0.63) 4.37 (±0.02) 2.04 (±0.02) 1.24 (±0.02) 72 1.01 (±0.29) 4.10 (±0.12) 1.01 (±0.29) 1.61 (±0.02) 3.52 (±0.27) 3.47 (±0.68) 1.63 (±0.02) 1.11 (±0.20)
Enterococcus faecalis EF37 showed the higher tyramine
pro-duction and tyrDC gene expression in the presence of tyrosine added to the media. In addition, independently on the media, E.
faecalis EF37 and E. faecium FC12 produced also high amount of
2-phenylethylamine, which were significantly higher in the pres-ence of tyrosine added. On the other hand, E. faecalis ATCC 29212 and E. faecium FC643 were not able to accumulate sig-nificantly 2-phenylethylamine when tyrosine was added; how-ever, the same strains produced this BA in reduced amounts in the absence of tyrosine in BHI if compared with the other two strains and in the same magnitude in the poor medium (BAM). The absence of 2-phenylethylamine in BAM and BHI
added with tyrosine and inoculated with E. faecalis ATCC 29212 and E. faecium FC643 reflected the lower efficiency of their tyrDC and could indicate that for these strains the increasing amount of tyramine can lower or inhibit further decarboxy-lase activities. Concerning transcriptional analysis, the mainte-nance of the tyrDC gene expression in the stationary phase of growth could contribute to enhance 2-phenylethylamine biosyn-thesis in enterococcal strains when the preferred precursor was depleted.
However, in the case of the strains E. faecalis ATCC 29212 and E. faecium FC643, that accumulated gradually tyramine, the tyrDC gene expression was still present at the end of the
incubation period, but 2-phenylethylamine was not produced because tyrosine was not entirely consumed after 72 h growth.
The early production of tyramine by E. faecalis EF37 and
E. faecium FC12 confirms the results ofPessione et al.(2009), who demonstrated that tyrDC activity in E. faecalis DISAV1022 reached its maximum level during the exponential growth phase, suggesting that tyrosine decarboxylation was not sim-ply a response to starvation or nutrient depletion typical of the stationary phase.
By contrast, the strains E. faecalis ATCC 29212 and E.
fae-cium FC643 accumulate great part of tyramine after they reached
the stationary phase, independently on the addition of precur-sor. However, these strains, although their transcript levels were much lower respect to E. faecalis EF37, showed a tyrDC tran-scription trend similar to E. faecalis EF37. In particular, these profiles, were characterized by an higher expression during the exponential phase followed by a decrease after 8 h of incubation.
Many authors reported the widespread ability of enterococci to produce both tyramine and 2-phenylethylamine (Beutling and Walter, 2002; Aymerich et al., 2006;Bonetta et al., 2008). This characteristic was found also in some lactobacilli (Landete et al., 2007), even if in other case a highly tyrosine selective tyrDC was described (Moreno-Arribas and Lonvaud-Funel, 2001).Marcobal et al. (2006) proved that tyrDC gene in E. faecium encoded for a functional and dual decarboxylase resulting in tyrosine and phenylalanine decarboxylation. Also Landete et al.(2007) demonstrated that tyrDC present in LAB allowed the produc-tion of 2-phenylethylamine. Pessione et al. (2009) carried out a comparative proteomic investigation on E. faecalis, which demonstrated a membrane bound tyrDC highly overexpressed during the production of both tyramine and 2-phenylethylamine. According to these authors, a yield of 100% was observed for the conversion of tyrosine, which takes place since the exponen-tial phase. On the other hand, the yield for 2-phenylethylamine was lower (about 10%) and its production occurred in the sta-tionary phase when tyrosine was exhausted. Also other authors observed that phenylalanine is decarboxylated with a reduced efficiency and only when the tyrosine become a limiting sub-strate (Joosten, 1988;Latorre-Moratalla et al., 2014). Regarding the different amount of tyramine accumulated under the same conditions, it has been demonstrated that the presence of high amounts of tyrosine in the medium can reduce the tyramine pro-duction by some LAB (Fernández et al., 2007). In other words, the increase in the availability of the precursor did not necessarily coincide with an increase in the decarboxylation.
The maximum yield for tyrosine conversion is 75.7%; then, in this study a stoichiometric conversion of the aminoacid added
should produce a maximum theoretical level of 609 g/l of tyra-mine. Taking into account that BHI without precursor supports the production of 70–90 mg/l of tyramine, the maximum accu-mulation of this BA showed by E. faecalis EF37 in the presence of tyrosine is lower than this theoretical limit (about 150 mg/l below). However, in these conditions a higher production of 2-phenylethylamine (150 mg/l above the yield in not supple-mented BHI) occurred. The overproduction of this BA was observed also in E. faecium FC12; however, in this case the results were reached in the presence of lower tyramine concen-tration. The same trend was also observed in BAM, in which E.
faecalis EF37 seems to operate an almost complete conversion
of the aromatic aminoacids added or naturally present in the medium.
Conclusion
The presence of Enterococcus strains that can decarboxylate tyro-sine and 2-phenylalanine is a serious concern in fermented food for consumer’s health. Indeed, even if these activities are com-mon acom-mong enterococci, this study underlines the extremely variable decarboxylating potential of strains belonging to the same species, suggesting strain-dependent implications in food safety. In spite of the fact that all the strains tested here had the
tyrDC gene, the amounts of tyramine (and 2-phenylethylamine)
produced was strictly dependent on the amount of its tran-scription, which was extremely different among the strains. The composition of the media also affected and modulated the amount and ratio of these BAs by tyraminogenic strains, indi-cating the need of preventive measures to control BAs accu-mulation in foods. Future researches will be planned to a deep knowledge on the conditions which can favor the production of BAs by enterococci and on the reasons which determine the important differences among the transcripts of the same gene. This could be ascribed to different activity and speci-ficity of tyrDC enzyme or to different regulation mechanisms. In this regards, further studies have to be performed to better explain the genetic and functional basis, and the environmen-tal factors affecting the different decarboxylating potential of the strains.
Acknowledgment
We acknowledge V. Prodomi for her valuable technical assis-tance.
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Conflict of Interest Statement: The authors declare that the research was con-ducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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